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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

3-Isoxazolecarboxaldehyde, 5-(4-fluorophenyl)-

O=Cc1noc(c1)c1ccc(cc1)F Request for Quotation
Chemical Name: 3-Isoxazolecarboxaldehyde, 5-(4-fluorophenyl)-
CAS Number: 640292-06-4
Product Number: AG003M5X(AGN-PC-00UQNC)
Synonyms:
MDL No:
Molecular Formula: C10H6FNO2
Molecular Weight: 191.1585

Identification/Properties

Computed Properties
Molecular Weight:
191.161g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
191.038g/mol
Monoisotopic Mass:
191.038g/mol
Topological Polar Surface Area:
43.1A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
204
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-(4-Fluorophenyl)isoxazole-3-carbaldehyde is a versatile compound that finds extensive application in chemical synthesis. Its unique structure and reactivity make it a valuable building block for the preparation of various organic compounds. Due to the presence of both an isoxazole ring and an aldehyde group, this compound exhibits diverse chemical properties that can be exploited in synthetic routes.One prominent application of 5-(4-Fluorophenyl)isoxazole-3-carbaldehyde is its use as a key intermediate in the synthesis of bioactive molecules and pharmaceuticals. The presence of the isoxazole ring imparts structural diversity and functionality to the molecules derived from it, making it a valuable scaffold for drug discovery and development. Additionally, the aldehyde group can serve as a versatile handle for further functionalization through various chemical reactions.In organic synthesis, 5-(4-Fluorophenyl)isoxazole-3-carbaldehyde can participate in a variety of transformations, such as condensation reactions, nucleophilic addition reactions, and heterocyclization reactions. These reactions can be utilized to introduce new functional groups, modify the structure, and enhance the properties of the target compounds. Overall, the versatility and reactivity of 5-(4-Fluorophenyl)isoxazole-3-carbaldehyde make it a valuable tool for chemists engaged in the synthesis of complex organic molecules.